Omeprazole

NDC 68382-500 · Zydus Pharmaceuticals USA Inc.

Generic nameOmeprazole

Dosage formCAPSULE, DELAYED RELEASE

RouteORAL

Active ingredient(s)OMEPRAZOLE

Strength40 mg/1

Pharmacologic classCytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]

Marketing categoryANDA

Packages

68382-500-01 — 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-500-01)

68382-500-05 — 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-500-05)

68382-500-06 — 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-500-06)

68382-500-10 — 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-500-10)

68382-500-16 — 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-500-16)

FDA lists these products with the same active ingredient.

68071-3007 — Omeprazole, 68071-3733 — Omeprazole, 68071-4024 — Omeprazole, 68071-4025 — omeprazole, 68071-4906 — omeprazole, 68084-128 — Omeprazole, 68196-700 — Omeprazole, 68196-915 — Omeprazole, 68382-411 — Omeprazole, 68382-412 — Omeprazole, 68391-103 — omeprazole, 68391-915 — Omeprazole, 68462-395 — Omeprazole, 68462-396 — Omeprazole, 68462-397 — Omeprazole, 68682-102 — omeprazole, sodium bicarbonate, 68682-104 — omeprazole, sodium bicarbonate, 68682-990 — omeprazole, sodium bicarbonate, 68788-4104 — Omeprazole, 68788-6881 — Omeprazole, +295 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.